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Compound Detail

CHEMBL1819286

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C[C@H]1O[C@H](O[C@H]2CC[C@@]3(C)[C@H](CC[C@@H]4[C@@H]3CC[C@]3(C)[C@@H](C5=CC(=O)OC5)CC[C@]43O)C2)[C@@H](O)[C@@H](O)[C@@H]1O

Basic Information

ChEMBL ID CHEMBL1819286
Phase Preclinical
Structure Type MOL
InChI Key WQMLFJWIKARBFW-HCGNMXHKSA-N
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

520.7
MW (Da)
2.46
ALogP
8
HBA
4
HBD
125.7
PSA (Ų)
0.33
QED
1
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C29H44O8
MW 520.66
Aromatic Rings 0
Heavy Atoms 37
NP-Likeness 3.05

Activity Summary

EC50 1 meas. best 7.58
IC50 1 meas. best 6.15

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human betaherpesvirus 5
CHEMBL371
EC50 7.58 7.58 26.6 1
NCI-H460
CHEMBL396
IC50 6.15 6.15 706.1 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
21660118 10.1021/ml100290d NCI-H460 9
24900847 10.1021/ml400529q HFF 2
24900847 10.1021/ml400529q Human betaherpesvirus 5 1
24900847 10.1021/ml400529q Unchecked 1

Data from ChEMBL 36 via Core Engine